Ganapathi T R, Higgs N S, Balint-Kurti P J, Arntzen C J, May G D, Van Eck J M
The Boyce Thompson Institute for Plant Research, Tower Road, Ithaca, NY 14853-1801, USA e-mail:
Plant Cell Rep. 2001 Feb;20(2):157-162. doi: 10.1007/s002990000287.
A protocol was developed for establishing embryogenic suspension cultures from in vitro-grown, thin shoot-tip sections of the banana cultivar Rasthali. The best medium for callus induction was an MS-based medium supplemented with 2 mg/l 2,4-D and 0.2 mg/l zeatin. The callus was transferred to liquid medium to establish embryogenic cell suspensions. These cultures were subsequently used for Agrobacterium-mediated transformation. The Agrobacterium tumefaciens strain EHA105 containing the binary vector pVGSUN with the als gene as a selectable marker and an intron-containing the gusA gene as a reporter gene was used for transformations. The herbicide Glean was used as a selection agent. Two hundred putative transformants were recovered, of which a set of 16 was tested by histochemical analysis for GUS expression and by Southern blot analysis with a probe for the gusA gene. The plants were positive for GUS expression and integration of the gusA gene. Two of the transformants were grown to maturity under greenhouse conditions. Bananas were harvested to test GUS expression by histochemical analysis. The fruit from both transgenics tested positive for GUS expression.
已制定了一项方案,用于从体外培养的香蕉品种Rasthali的嫩茎尖切片建立胚性悬浮培养物。诱导愈伤组织的最佳培养基是添加了2 mg/l 2,4-D和0.2 mg/l玉米素的基于MS的培养基。将愈伤组织转移至液体培养基中以建立胚性细胞悬浮培养物。这些培养物随后用于农杆菌介导的转化。含有二元载体pVGSUN的根癌农杆菌菌株EHA105,其中als基因作为选择标记,含内含子的gusA基因作为报告基因,用于转化。除草剂Glean用作选择剂。共获得200个推定转化体,其中一组16个通过组织化学分析检测GUS表达,并使用gusA基因探针进行Southern印迹分析。这些植株GUS表达和gusA基因整合均呈阳性。其中两个转化体在温室条件下生长至成熟。收获香蕉以通过组织化学分析检测GUS表达。两个转基因植株的果实GUS表达均呈阳性。